BDBM14008 (11R)-32-oxo-25-oxa-8,12,16,18-tetraazahexacyclo[24.3.1.1^{8,11}.1^{20,24}.0^{2,7}.0^{14,18}]dotriaconta-1(30),2,4,6,14,16,20(31),21,23,26,28-undecaene-23-carbonitrile::(23R)-22,23,24,25-Tetrahydro-22-oxo-16H,21H-21,23-ethano-6,10:12,16-dimethenobenz[g]-imidazo[4,3-n][1,9,12,15]oxatriazacycloheneicosine-9-carbonitrile::CHEMBL524862::Macrocyclic 3-Aminopyrrolidinone analog 42

SMILES O=C1[C@H]2CCN1c1ccccc1-c1cccc(Oc3cc(Cn4cncc4CN2)ccc3C#N)c1

InChI Key InChIKey=BDXLTTUQHGMFEE-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 14008   

LigandPNGBDBM14008((23R)-22,23,24,25-Tetrahydro-22-oxo-16H,21H-21,23-...)
Affinity DataIC50: 1.30nMpH: 7.5 T: 2°CAssay Description:Compounds were tested as inhibitors of FTase in vitro using purified recombinant human enzyme to catalyze the reaction between [3H]FPP and a recombin...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/27/2007
Entry Details Article
PubMed
LigandPNGBDBM14008((23R)-22,23,24,25-Tetrahydro-22-oxo-16H,21H-21,23-...)
Affinity DataIC50: 810nMAssay Description:Compounds were tested as inhibitors of FTase in vitro using purified recombinant human enzyme to catalyze the reaction between [3H]FPP and a recombin...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/27/2007
Entry Details Article
PubMed
LigandPNGBDBM14008((23R)-22,23,24,25-Tetrahydro-22-oxo-16H,21H-21,23-...)
Affinity DataIC50: 2.60E+3nMAssay Description:Inhibition of human ERG channelMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/23/2012
Entry Details Article
PubMed